Clinical Research Coordinator A
About The Position
This position will assist in the management of multiple clinical trials and responsibilities in specific research area. Coordinate the screening of patients, subject enrollment, collection and storage of biological samples and related study documents, and collection of clinical data. Assist with Institutional Review Board (IRB) filings and inquiries, and assist in the preparation of manuscripts, grant proposals, and research related presentations. Works closely with the Principal Investigator, manager, and study team to identify problems and develop solutions. Implement approved changes to procedures as needed and monitor results. Responsible for study coordination for investigator-initiated studies, multi-center research studies, and patient-oriented clinical and translational research projects.
Requirements
- Bachelor of Science and 1 to 2 years of experience or equivalent combination of education and experience is required.
- This position is cogentin upon funding
Responsibilities
- Conduct clinical investigation utilizing GCP, which includes possessing and demonstrating knowledge of federal regulations and guidance documents for the conduct of clinical studies involving human subject and their protection.
- Assure compliance with the protocol and regulatory requirements includes: collecting, recording, and maintaining data and source documentation and maintaining regulatory binders through subject study completion.
- Coordinate and conduct human subject clinical study including: subject recruitment; visit scheduling and facilitation; informed consent; case report form population; chart maintenance; data management.
- Accurate and timely database inputting, management and analysis based upon source documentation.
- General organization, maintenance, ordering and stocking supplies, maintaining equipment required to conduct study.
- Coordinate with team members in retrieval and provision of documentation required for IRB submission/renewals in accordance with guidelines; continuing review, modification, deviation, adverse events, etc.
- Conduction of intermittent telephone contact with potential and current study participants in fulfillment of protocol requirements.
- Meticulous documentation and reporting of all study and recruitment procedures and human subject interactions ongoing throughout research study.
- Attendance at and active participation in weekly team meetings, responsive to Investigators and accurate in reporting throughout investigation.
- Perform additional duties as assigned.
Benefits
- excellent healthcare
- tuition benefits for employees and their families
- generous retirement benefits
- a wide variety of professional development opportunities
- supportive work and family benefits
- a wealth of health and wellness programs and resources
- Health, Life, and Flexible Spending Accounts
- comprehensive medical, prescription, behavioral health, dental, vision, and life insurance benefits
- flexible spending accounts to pay for eligible health care and dependent care expenses with pre-tax dollars
- exceptional tuition benefits
- tuition assistance here at Penn
- tuition assistance at other institutions for dependent children
- generous retirement plans
- Penn’s Basic, Matching, and Supplemental retirement plans
- save for retirement on a pre-tax or Roth basis
- wide variety of investment options through TIAA and Vanguard
- substantial amount of time away from work
- Long-Term Care Insurance
- wellness and work-life resources
- Professional and Personal Development
- access to a wide range of University resources as well as cultural and recreational activities
- Discounts and Special Services
- Flexible Work Hours
- Penn Home Ownership Services
- Adoption Assistance
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
